A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism-Reference-Cited by-同舟云学术

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism

Published:2006-08-13 Issue:9 Volume:38 Page:999-1001
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Koolen David A,Vissers Lisenka E L M,Pfundt Rolph,de Leeuw Nicole,Knight Samantha JL,Regan Regina,Kooy R Frank,Reyniers Edwin,Romano Corrado,Fichera Marco,Schinzel Albert,Baumer Alessandra,Anderlid Britt-Marie,Schoumans Jacqueline,Knoers Nine V,van Kessel Ad Geurts,Sistermans Erik A,Veltman Joris A,Brunner Han G,de Vries Bert B A

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1853.pdf

Reference15 articles.

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2. de Vries, B.B. et al. Am. J. Hum. Genet. 77, 606–616 (2005).

3. Schouten, J.P. et al. Nucleic Acids Res. 30, e57 (2002).

4. Stefansson, H. et al. Nat. Genet. 37, 129–137 (2005).

5. Lupski, J.R. Trends Genet. 14, 417–422 (1998).

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